# autosomal recessive nonsyndromic deafness 7

> autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the TMC1 gene on chromosome 9q21

**Wikidata**: [Q28024647](https://www.wikidata.org/wiki/Q28024647)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-7


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/5658)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGCIEX:assertion_5658)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)